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441330-00-3

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  • (3,4,5,6-TETRAHYDRO-2H-[1,4']BIPYRIDINYL-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER

    Cas No: 441330-00-3

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441330-00-3 Usage

Description

(3,4,5,6-TETRAHYDRO-2H-[1,4']BIPYRIDINYL-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER is a carbamic acid derivative with the molecular formula C19H26N2O2, belonging to the class of organic compounds known as phenylpyridines. (3,4,5,6-TETRAHYDRO-2H-[1,4']BIPYRIDINYL-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER is characterized by its tert-butyl ester group, which provides stability and makes it a suitable candidate for drug development.
Used in Pharmaceutical Industry:
(3,4,5,6-TETRAHYDRO-2H-[1,4']BIPYRIDINYL-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER is used as a therapeutic agent for its potential in treating various health conditions. Its stability and unique structure make it a promising candidate for further investigation and development as a medication.
Used in Research:
(3,4,5,6-TETRAHYDRO-2H-[1,4']BIPYRIDINYL-4-YL)-CARBAMIC ACID TERT-BUTYL ESTER is used as a research compound to explore its potential applications and properties in the field of medicinal chemistry. Its unique structure and stability contribute to its value as a subject for scientific study.

Check Digit Verification of cas no

The CAS Registry Mumber 441330-00-3 includes 9 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 6 digits, 4,4,1,3,3 and 0 respectively; the second part has 2 digits, 0 and 0 respectively.
Calculate Digit Verification of CAS Registry Number 441330-00:
(8*4)+(7*4)+(6*1)+(5*3)+(4*3)+(3*0)+(2*0)+(1*0)=93
93 % 10 = 3
So 441330-00-3 is a valid CAS Registry Number.

441330-00-3Relevant articles and documents

Novel factor Xa inhibitors based on a 2-carboxyindole scaffold: SAR of P4 substituents in combination with a neutral P1 ligand

Nazare, Marc,Essrich, Melanie,Will, David W.,Matter, Hans,Ritter, Kurt,Urmann, Matthias,Bauer, Armin,Schreuder, Herman,Czech, Joerg,Lorenz, Martin,Laux, Volker,Wehner, Volkmar

, p. 4197 - 4201 (2007/10/03)

A series of novel, highly potent 2-carboxyindole-based factor Xa inhibitors is described. Structural requirements for P4 ligands in combination with a neutral biaryl P1 ligand were investigated with the 2-carboxyindole scaffold. A diverse set of P4 substituents was identified, which, in conjunction with a biaryl P1 ligand, gave highly potent factor Xa inhibitors, which were also selective versus other proteases and efficacious in various antithrombotic secondary assays.

Inhibitors of factor Xa

-

, (2008/06/13)

Novel compounds, their salts and compositions related thereto having activity against mammalian factor Xa are disclosed. The compounds are useful in vitro or in vivo for preventing or treating coagulation disorders.

Inhibitors of factor Xa

-

, (2008/06/13)

Novel compounds, their salts and compositions related thereto having activity against mammalian factor Xa are disclosed. The compounds are useful in vitro or in vivo for preventing or treating coagulation disorders.

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